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脊髓损伤大鼠膀胱传入神经元兴奋性增高与 Kv1.4α 亚单位减少有关。

Hyperexcitability of bladder afferent neurons associated with reduction of Kv1.4 α-subunit in rats with spinal cord injury.

机构信息

Department of Urology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; Department of Urology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

J Urol. 2013 Dec;190(6):2296-304. doi: 10.1016/j.juro.2013.07.058. Epub 2013 Jul 27.

Abstract

PURPOSE

To clarify the functional and molecular mechanisms inducing hyperexcitability of C-fiber bladder afferent pathways after spinal cord injury we examined changes in the electrophysiological properties of bladder afferent neurons, focusing especially on voltage-gated K channels.

MATERIALS AND METHODS

Freshly dissociated L6-S1 dorsal root ganglion neurons were prepared from female spinal intact and spinal transected (T9-T10 transection) Sprague Dawley® rats. Whole cell patch clamp recordings were performed on individual bladder afferent neurons. Kv1.2 and Kv1.4 α-subunit expression levels were also evaluated by immunohistochemical and real-time polymerase chain reaction methods.

RESULTS

Capsaicin sensitive bladder afferent neurons from spinal transected rats showed increased cell excitability, as evidenced by lower spike activation thresholds and a tonic firing pattern. The peak density of transient A-type K+ currents in capsaicin sensitive bladder afferent neurons from spinal transected rats was significantly less than that from spinal intact rats. Also, the KA current inactivation curve was displaced to more hyperpolarized levels after spinal transection. The protein and mRNA expression of Kv1.4 α-subunits, which can form transient A-type K+ channels, was decreased in bladder afferent neurons after spinal transection.

CONCLUSIONS

Results indicate that the excitability of capsaicin sensitive C-fiber bladder afferent neurons is increased in association with reductions in transient A-type K+ current density and Kv1.4 α-subunit expression in injured rats. Thus, the Kv1.4 α-subunit could be a molecular target for treating overactive bladder due to neurogenic detrusor overactivity.

摘要

目的

为了阐明脊髓损伤后 C 纤维膀胱传入通路兴奋过度的功能和分子机制,我们研究了膀胱传入神经元电生理特性的变化,特别关注电压门控钾通道。

材料和方法

从雌性脊髓完整和脊髓横切(T9-T10 横切)的 Sprague Dawley®大鼠的 L6-S1 背根神经节中分离出新鲜的背根神经节神经元。对单个膀胱传入神经元进行全细胞膜片钳记录。还通过免疫组织化学和实时聚合酶链反应方法评估 Kv1.2 和 Kv1.4α亚基表达水平。

结果

来自脊髓横切大鼠的辣椒素敏感膀胱传入神经元表现出更高的细胞兴奋性,这表现在更低的峰激活阈值和紧张性放电模式。来自脊髓横切大鼠的辣椒素敏感膀胱传入神经元的短暂 A 型 K+电流的峰值密度明显小于脊髓完整大鼠。此外,脊髓横切后 KA 电流失活曲线向更超极化水平移位。脊髓横切后,膀胱传入神经元中形成短暂 A 型 K+通道的 Kv1.4α亚基的蛋白和 mRNA 表达减少。

结论

结果表明,与脊髓完整大鼠相比,损伤大鼠中辣椒素敏感 C 纤维膀胱传入神经元的兴奋性增加,与短暂 A 型 K+电流密度和 Kv1.4α亚基表达减少有关。因此,Kv1.4α亚基可能成为治疗神经源性逼尿肌过度活动引起的逼尿肌过度活动的分子靶点。

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